Hays AP - Search Results

1

Becker muscular dystrophy or spinal muscular atrophy?--Dystrophin studies resolve conflicting results of electromyography and muscle biopsy.

McDonald TD, Medori R, Younger DS, Chang HW, Minetti C, Uncini A, Bonilla E, Hays AP, Lovelace RE. McDonald TD, et al. Among authors: hays ap. Neuromuscul Disord. 1991;1(3):195-200. doi: 10.1016/0960-8966(91)90024-m. Neuromuscul Disord. 1991. PMID: 1822794

2

Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.

Bonilla E, Schmidt B, Samitt CE, Miranda AF, Hays AP, de Oliveira AB, Chang HW, Servidei S, Ricci E, Younger DS, et al. Bonilla E, et al. Among authors: hays ap. Am J Pathol. 1988 Dec;133(3):440-5. Am J Pathol. 1988. PMID: 3059802 Free PMC article.

3

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder.

Hirano M, Silvestri G, Blake DM, Lombes A, Minetti C, Bonilla E, Hays AP, Lovelace RE, Butler I, Bertorini TE, et al. Hirano M, et al. Among authors: hays ap. Neurology. 1994 Apr;44(4):721-7. doi: 10.1212/wnl.44.4.721. Neurology. 1994. PMID: 8164833

4

Erroneous diagnosis corrected after 28 years. Not spinal muscular atrophy with ophthalmoplegia but minicore myopathy.

Gordon PH, Hays AP, Rowland LP, Dickoff DJ, Schotland DL, Rosenberg RN, Wolfe DE, Lange DJ, Lovelace RE. Gordon PH, et al. Among authors: hays ap. Arch Neurol. 1996 Nov;53(11):1194-6. doi: 10.1001/archneur.1996.00550110146028. Arch Neurol. 1996. PMID: 8912497

5

Multifocal motor neuropathy with conduction block: is it a distinct clinical entity?

Lange DJ, Trojaborg W, Latov N, Hays AP, Younger DS, Uncini A, Blake DM, Hirano M, Burns SM, Lovelace RE, et al. Lange DJ, et al. Among authors: hays ap. Neurology. 1992 Mar;42(3 Pt 1):497-505. doi: 10.1212/wnl.42.3.497. Neurology. 1992. PMID: 1549208

6

Long-duration polyphasic motor unit potentials in myopathies: a quantitative study with pathological correlation.

Uncini A, Lange DJ, Lovelace RE, Solomon M, Hays AP. Uncini A, et al. Among authors: hays ap. Muscle Nerve. 1990 Mar;13(3):263-7. doi: 10.1002/mus.880130315. Muscle Nerve. 1990. PMID: 2320048

7

Motor neuron disease and amyotrophic lateral sclerosis: relation of high CSF protein content to paraproteinemia and clinical syndromes.

Younger DS, Rowland LP, Latov N, Sherman W, Pesce M, Lange DJ, Trojaborg W, Miller JR, Lovelace RE, Hays AP, et al. Younger DS, et al. Among authors: hays ap. Neurology. 1990 Apr;40(4):595-9. doi: 10.1212/wnl.40.4.595. Neurology. 1990. PMID: 2320231

8

Recurrent myoglobinuria and HIV seropositivity: incidental or pathogenic association?

Younger DS, Hays AP, Uncini A, Lange DJ, Lovelace RE, DiMauro S. Younger DS, et al. Among authors: hays ap. Muscle Nerve. 1989 Oct;12(10):842-3. doi: 10.1002/mus.880121009. Muscle Nerve. 1989. PMID: 2608081

9

The neuromuscular manifestations of human immunodeficiency virus infections.

Lange DJ, Britton CB, Younger DS, Hays AP. Lange DJ, et al. Among authors: hays ap. Arch Neurol. 1988 Oct;45(10):1084-8. doi: 10.1001/archneur.1988.00520340038008. Arch Neurol. 1988. PMID: 2845898

10

Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface.

Bonilla E, Samitt CE, Miranda AF, Hays AP, Salviati G, DiMauro S, Kunkel LM, Hoffman EP, Rowland LP. Bonilla E, et al. Among authors: hays ap. Cell. 1988 Aug 12;54(4):447-52. doi: 10.1016/0092-8674(88)90065-7. Cell. 1988. PMID: 3042151

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